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Pharmacogenomic Studies of Current Antidiabetic Agents and Potential New Drug Targets for Precision Medicine of Diabetes

机译:目前抗糖尿病药物研究和糖尿病精密药物潜在新药物靶标的研究

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摘要

The pharmacokinetic process of metformin and the potential effect of its pharmacogenomic genes. After entering the gastrointestinal tract, metformin in intestinal endothelium is absorbed into intestinal epithelial cells by PMAT (encoded by SLC29A4) and OCT3 (encoded by SLC22A3), and transported into blood by OCT1 (encoded by SLC22A1). When metformin gets to the liver, OCT1 and OCT3 in membranes of hepatocytes take it up, and MATE1 (encoded by SLC47A1) transports it into the liver where it is ultimately eliminated with bile. Metformin also is taken up into epithelial cells of the kidney by OCT2 (encoded by SLC22A2). MATE1 and MATE2 (encoded by SLC47A2) are responsible for excretion of metformin into urine
机译:二甲双胍的药代动力学过程及其药物基因基因的潜在效应。进入胃肠道后,通过PMAT(由SLC29A4)和OCT3(由SLC22A3编码)(由SLC22A3编码)吸收到肠上皮细胞中的二甲双胍,并在OCT1(由SLC22A1编码)进入血液中。当二甲双胍进入肝脏时,肝细胞膜中的Oct1和Oct3将其采用,并且Mate1(由SLC47A1编码)将其传送到肝脏中,在那里它最终用胆汁消除。二甲双胍也被OCT2溶于肾的上皮细胞(由SLC22A2编码)。 mate1和mate2(由slc47a2编码)负责石英素的排泄到尿液中

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